Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

CHILD syndrome

MONDO:0010621

CHILD syndrome (Congenital Hemidysplasia with Ichthyosiform nevus and Limb Defects, CS) is an X-linked dominant genodermatosis characterized by unilateral inflammatory and scaling skin lesions with ipsilateral visceral and limb anomalies.

Also known as: CHILD syndrome, CHILD syndrome, X-linked dominant, Ichthyosis, CHILD Syndrome, child nevus, child syndrome, congenital hemidysplasia with ichthyosiform erythroderma and limb defects, congenital hemidysplasia with ichthyosiform nevus and limb defects, ichthyosiform erythroderma, unilateral, with ipsilateral malformations, especially absence deformity of limbs

1480 clinical trials for this condition and its sub-types, 37 tagged with CHILD syndrome itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →
Sort by

Showing the 400 most recently updated of 723 trials in this tab.